Blood Pressure Lowering Effects of Angiotensin-(1-7) in Primary Autonomic Failure

Pure Autonomic Failure Clinical Trial

Official title: Blood Pressure Lowering Effects of Angiotensin-(1-7) in Primary Autonomic Failure

Status Terminated

Clinical Trial Summary

Pharmacologic approaches to increase levels or actions of the vasodilatory peptide angiotensin-(1-7) are currently in development for the treatment of hypertension based on findings from animal models. There are limited and contradictory clinical studies, however, and it is not clear if this peptide regulates blood pressure in humans. The purpose of this study is to better understand the cardiovascular effects angiotensin-(1-7) in human hypertension, and to examine interactions of this peptide with the autonomic nervous system. The investigators propose that the difficulties in showing angiotensin-(1-7) cardiovascular effects in previous clinical studies relates to the buffering capacity of the baroreceptor reflex to prevent changes in blood pressure. Autonomic failure provides the ideal patient population to test this hypothesis. These patients have loss of baroreflex buffering and have low levels of angiotensin-(1-7) in blood. The investigators will test if angiotensin-(1-7) infusion can lower blood pressure in patients with autonomic failure, and will determine the hemodynamic and hormonal mechanisms involved in this effect.

Clinical Trial Description

This is an inpatient study that requires at least four days of admission to the Vanderbilt Clinical Research Center. Autonomic failure patients will be placed on a fixed diet during the admission and will have routine tests performed for screening and clinical characterization. Patients will then receive intravenous angiotensin-(1-7) or saline infusion on two separate study days, with each study day lasting approximately 3 hours. There will be at least one washout day between study days. Patients will be instrumented with two intravenous catheters (one for blood sampling and one for drug infusion), arm and finger blood pressure cuffs, and sticky patches to measure heart rate during the study. The investigators will take baseline measurements of blood pressure and heart rate and collect blood samples. The investigators will also perform a rebreathing test to measure the heart's pumping capacity. After baseline measurements, the investigators will infusion angiotensin-(1-7) or saline for 50 minutes. There will be five doses of angiotensin-(1-7). Each dose will be maintained for 10 minutes. The investigators will measure blood pressure and heart rate, repeat the rebreathing test, and collect blood samples at the end of each dosing period. ;

Related Conditions & MeSH terms

• Autonomic Nervous System Diseases
• Autonomic Nervous System Disorders
• Hypotension
• Hypotension, Orthostatic
• Multiple System Atrophy
• Nervous System Diseases
• Orthostatic Hypotension, Dysautonomic
• Primary Dysautonomias
• Pure Autonomic Failure
• Shy-Drager Syndrome

• NCT number: NCT02591173
• Study type: Interventional
• Source: Vanderbilt University Medical Center
• Status: Terminated
• Phase: Early Phase 1
• Start date: February 2016
• Completion date: July 2020